ClinVar Miner

List of variants in gene CDAN1 reported as likely benign for anemia (disease)

Included ClinVar conditions (263):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 12
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HGVS dbSNP
NM_138477.4(CDAN1):c.*463_*465del rs111961345
NM_138477.4(CDAN1):c.157C>T (p.Leu53=) rs186189866
NM_138477.4(CDAN1):c.1968C>T (p.Thr656=) rs61742992
NM_138477.4(CDAN1):c.1969G>A (p.Gly657Ser) rs61747153
NM_138477.4(CDAN1):c.2445C>T (p.Gly815=) rs114208791
NM_138477.4(CDAN1):c.2836C>T (p.Arg946Trp) rs114779238
NM_138477.4(CDAN1):c.2948-13C>T rs117946783
NM_138477.4(CDAN1):c.3194G>A (p.Arg1065Gln) rs61746356
NM_138477.4(CDAN1):c.3450+11C>T rs56046122
NM_138477.4(CDAN1):c.386G>A (p.Arg129His) rs12441516
NM_138477.4(CDAN1):c.558C>G (p.Pro186=) rs12594325
NM_138477.4(CDAN1):c.816C>A (p.Thr272=) rs76599133

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